• 폴리머
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• 제24권5호
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• pp.599-609
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• 2000

본 연구에서는 불포화 폴리에스테르 수지의 기계적 물성을 증진시키기 위하여 프로필렌글리콜(PG)과 네오펜틸글리콜(NPG)의 몰비를 달리한 불포화 폴리에스테르 수지를 제조하여 경화거동 및 기계적 물성을 조사하였다. 경화거동은 microgel reaction mechanism을 이용하여 설명하였고, NPG 몰비의 증가는 최종 전화율을 증가시키나 경화속도가 늦어짐을 알 수 있었다. 그리고 글리콜 몰비중에서 NPG 몰비의 증가는 굴곡강도, 인장탄성율, 흡수율, 함침성이 증가하였고, 반면에 인장강도, 신율, 굴곡탄성율이 감소하는 경향으로 나타났다. 따라서 중합한 불포화 폴리에스테르 수지에서 PG/NPG 몰비가 0.5/0.5, 0.25/0.75의 영역일 때 섬유강화 플라스틱 복합재료의 물성이 우수한 것으로 관찰되었다.

• 한국응용과학기술학회지
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• 제25권1호
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• pp.1-14
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• 2008

To prepare weather-resistant modified silane acrylic resin coatings for an architectural purpose, tetrapolymers were synthesized by radical polymerization. 3-Methacryloxypropyltrimethoxysilane (MPTS) as a silicone monomer and n-butyl acrylate, methyl methacrylate, and n-butyl methacrylate as acrylic monomers were used. The composition of monomers was adjusted to fix the glass transition temperature of acrylic polymer for $20^{\circ}C$. The composition of MPTS in the synthesized polymer were varied from 10 wt% to 30 wt%. On the basis of synthesized resin amber paints were prepared and their physical properties and effects on weatherability were examined. The presence of MPTS in modified silane acrylic resins generally resulted in low molecular weight and broad molecular weight distribution, and also lowered the viscosity of the copolymers. The coated films prepared from these resins showed good and balanced properties in general. Adhesion to the substrate was outstanding in particular. Weatherability tests were carried out in three different types such as outdoor exposure, QUV, and SWO. The test results showed that the modified silane acrylic resins containing 30 wt% of MPTS had superior weathering properties.

• 대한화학회지
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• 제29권3호
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• pp.283-286
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• 1985

비다공성 및 다공성 4-비닐피리딘디비닐벤젠 이온교환수지를, 서스펜션 중합방법으로 합성하였다. 합성한 이들 수지들은 적외선 흡수스펙트럼을 통하여 확인하였다. 다공성수지의 세공용적과 세공스펙트럼들은 수은 Porosimeter를 사용하여 측정하였다. 다공성 4-비닐피리딘디비닐벤젠 이온교환수지, P-4VPDVB, 50-100 mesh의 세공용적과 세공크기에 미치는 diluent와 %DVB의 영향이 논의되었다. 그리고 이들 비다공성 및 다공성 4-비닐피리딘 디비닐벤젠 수지들의 이온교환용량은 5.0meq/g이었다.

• Restorative Dentistry and Endodontics
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• 제17권1호
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• pp.181-190
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• 1992

The purpose of this study was to estimate the contents of the residual monomers, such as Bis-GMA and TEGDMA. In this study, materials used were six kinds of anterior and posterior visible light-cured resins. Resins were placed in disk-shaped Teflon mold (8.5mm in diameter, 2.0mm in thickness), and cured for 20 seconds with visible light source attached wide diameter lightguide. The specimens were immersed in 10ml ethanol and stored for 5 days at $37^{\circ}C$. The concentration of residual monomers in eluate solution was analysed by HPLC, and the following results are obtained. 1. The residual Bis-GMA and TEGDMA were detected in all materials used, and the ranges of quantity of the residual Bis-GMA was 0.101-1.236 wt% and that of TEGDMA was 0.230-5.794 wt%.2. The contents of residual TEGDMA was detected higher than that of residual Bis-GMA (P < 0.01). 3. The content of residual monomers was detected to be highest in Bis-Fil M as microfilled type. 4. In most of the materials used, there was no significant difference in the contents of residual monomers between anterior and posterior light-cured resins.

• Restorative Dentistry and Endodontics
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• 제19권1호
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• pp.194-204
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• 1994

The purpose of this study was to evaluate the surface hardness of composite resins according to heat treatment. storage condition and storage time. In this study. two kinds of composite resin inlays and one kind of conventional posterior composite resin were used as experimental materials. One hundred eighty composite resin specimens were constructed from composite resin inlays and conventional posterior composite resin. The conditions of this study were heat treatment. storage condition and storage time. Hardness readings were taken from the top surface of each samples using the Vickers microhardness tester(MHT-l. Matsuzawa. Japan}. The following results from this study were obtained: 1. Regardless of storage condition. both composite resin inlay and conventional posterior composite resin have a higher surface hardness under heat treatment than not. 2. Composite resins with heat treatment have a higher surface hardness under dry storage than under water immersion. 3. In case of Clearfil Photo Posterior and Brilliant Enamel with heat treatment. there was no significant difference with time. but Clearfil CR Inlay with heat treatment. there was statistical difference after 24 hours. 4. Surface hardness of composite resins with coarse hybrid type was higher than that of composite resin with fine hybrid type.

• Macromolecular Research
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• 제10권6호
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• pp.332-338
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• 2002

The effect of an electron beam and ${\gamma}$-ray irradiation on the curing of epoxy resins was investigated. Diglycidyl ether of bisphenol A (DGEBA) and diglycidyl ether of bisphenol F (DGEBF) as epoxy resin were used. The epoxy resins containing 1.0-3.() wt% of triarylsulphonium hexafluoroantimonate(TASHFA) and triarylsulphonium hexafluorophosphate(TASHFP) as initiator were irradiated under nitrogen at room temperature with different dosage of EB and ${\gamma}$-rays from a Co$^{60}$ u source. The chemical and mechanical characteristics of irradiated epoxy resins were compared after curing of EB and ${\gamma}$-ray irradiation. The thermal properties of cured epoxy were investigated using dynamic mechanical thermal analysis. The chemical structures of cured epoxy were characterized using near infrared spectroscopy. Mechanical properties such as flexural strength, modulus were measured. The gel fraction of DGEBA with ${\gamma}$-ray was higher than that of the epoxy with EB at the same dose. Young's modulus of the sample irradiated by ${\gamma}$-ray is higher than that of sample cured by EB. From the result of strain at yield, it was found that the epoxy cured by ${\gamma}$-ray had a higher stiff property compared with the irradiated by EB.

• 소성∙가공
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• 제13권6호
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• pp.515-521
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• 2004

The shrinkages of injection molded parts are different in molding operational conditions and mold design. It also differs from resins. The shrinkages of injection molded parts fur PBT (polybutylene terephthalate), PC (polycarbonate), and glass reinforced PBT and PC have been studied for various operational conditions of injection molding. The part shrinkage of crystalline polymer, PBT was higher than that of amorphous polymer, PC by about two times. The part shrinkages of both polymers decreased as glass fiber content increases. Higher injection temperature and lower injection pressure resulted in a higher shrinkage in both PBT and PC resins. As mold temperature increases the part shrinkage of PC decreased. However, the part shrinkage of PBT increased as mold temperature increases. The part shrinkages of PBT and PC resins decreased as gate size increases since the pressure delivery is mush easier for a larger gate size. The part shrinkage of flow direction was less than that of the perpendicular direction to the flow for both pure and glass fiber reinforced resins. The part shrinkage at the position close to the gate was less than that of the position far from the gate.

• Restorative Dentistry and Endodontics
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• 제12권2호
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• pp.33-44
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• 1987

The use of composite resin for the posterior teeth gives rise to clinical problem due to the lack of mechanical properties. The purpose of this study was to observe the fractured surfaces of light posterior composite resins which are P-10, Clearfil posterior, Adaptic anterior & posterior, P-30, Lite-fil posterior, Estilux posterior, Helio-molar, and Ful-fil com pules (Table 1). The failure of composite resin specimens of I, T and Y-Type (Fig. 1,2) occured under compression. Fractographical observations by SEM (JSM-T20, JEOL) were carried out in order to examine the fracture behaviour of eight composite resins in different types of specimens. The results obtained from this study were as follows: 1. Similar features were found in fractured surfaces of eight composite resins. 2. The crack growth was initiated at the regions of porosities. 3. The crack propagated on the filler-matrix interface. 4. As the crack increased in size, it accelerated to form secondary crack. 5. The fracture behaviour was dependent on the content, size, shape, and distribution of fillers.

• 방사선산업학회지
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• 제4권1호
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• pp.19-23
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• 2010

Vinyl ester (VE) resins, introduced in the late 1960s, have made large strides in reinforced plastics applications as adhesive and matrix materials on their appropriate mechanical performance characteristics in the glassy state. Generally, VE resins are a group of dimethacrylate resins based on bisphenol A type epoxy resin. They exhibit easy handling properties as well as good resistance to most chemical agents due to their mechanical and thermal properties. In this study, the effects of curing methods of vinyl ester resins on gel contents, flexural strength and dynamic mechanical properties were investigated. Thermal curing (room temperature, $80^{\circ}C$) and electron beam curing were used to crosslink a VE resin/styrene complex (65/35 wt%) with methyl ethyl ketone peroxide (MEKPO) as a catalyst and an 8 wt% cobalt naphthenate in styrene solution as a accelerator. For the samples, gel contents as well as flexural strength and dynamic mechanical properties were characterized and compared by soxhlet apparatus, universal testing machine (UTM) and dynamic mechanical analysis (DMA). As a result, the electron-cured VE resin was confirmed as a better condition than those for gel contents, flexural strength and dynamic mechanical properties, respectively.

• Macromolecular Research
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• 제17권11호
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• pp.870-873
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• 2009

In this study, 2-diglycidylether of benzotrifluoride (2-DGEBTF) and 4-diglycidylether of benzotrifluoride (4-DGEBTF) epoxy resins, which contained fluorine groups in the main chain, were synthesized. The resins were characterized by FTIR, $^1H$ NMR, $^{13}C$ NMR and $^{19}F$ NMR spectroscopy. The 2-DGEBTF and 4-DGEBTF epoxy resins were cured with triethylene tetramine (TETA), and the effect of the fluorine group on the synthesized epoxy resin on the cure behavior, thermal, and mechanical properties was investigated. The 2-DGEBTF/TETA system was more reactive than the 4-DGEBTF/TETA system, whereas the thermal stability factor i.e., the decomposition activation energy ($E_d$), of 4-DGEBTF/TETA was higher than that of 2-DGEBTF/TETA. These results can be explained by the decrease in cross-linking density and decomposition of the short side chains, resulting in the $CF_3$ group at the para position. However, the $K_{IC}$ value of 4-DGEBTF/TETA was higher than that of 2-DGEBTF/TETA. This was attributed to the increase in flexibility in the epoxy backbone, resulting in a difference in steric hindrance and polarlizability.